Abelson Abby
Center for Osteoporosis and Metabolic Bone Disease, Department of Rheumatic and Immunologic Diseases, Orthopaedic and Rheumatology Institute, The Cleveland Clinic, Cleveland, OH 44195, USA.
Curr Med Res Opin. 2008 Mar;24(3):695-705. doi: 10.1185/030079908X260899. Epub 2008 Jan 25.
Paget's disease of bone, the second most common metabolic bone disease in the United States, is characterized by localized areas of excessive bone resorption coupled with accelerated bone formation, resulting in new bone that is less structurally organized and is weaker than normal bone. Complications of Paget's disease can include bone pain, osteoarthritis, skeletal deformity, hearing loss, and fractures. The objective of this review is to provide a comprehensive overview of current standards of treatment in Paget's disease.
A review of literature from 1974 to 2007 was performed on topics such as epidemiology, etiology, treatment of Paget's disease of bone, and bisphosphonates.
Paget's disease affects an estimated 2-7% of persons of age 55 years or older in North America and western Europe. Antiresorptive treatment with bisphosphonates is the standard treatment, but there may be limitations to oral therapy. Intravenous pamidronate is efficacious and has long been available, but its use is hindered by an impractical recommended dosing regimen of 30 mg IV over 4 h for three consecutive days. In two identical, double-blind, 6-month trials, 96% of patients treated with a one-time intravenous treatment of zoledronic acid 5 mg achieved therapeutic response, compared with 74% treated with 60 days of daily oral treatment with risedronate 30 mg (p < 0.001). One limitation of this review is that historical data are not reviewed in the same level of detail as newer treatments, because recent advances in pharmacotherapy of Paget's disease have reduced the clinical utility of the older drugs.
The etiology of Paget's disease is unclear, but some evidence suggests genetic and viral components. Bisphosphonates restore normal bone turnover and relieve bone pain, but oral formulations may be limited by complicated dosing regimens and poor gastrointestinal absorption. The bisphosphonate, zoledronic acid is administered as a single intravenous infusion and offers antiresorptive efficacy and longer-lasting remission.
骨佩吉特病是美国第二常见的代谢性骨病,其特征是局部骨吸收过多,同时骨形成加速,导致新形成的骨结构组织较差且比正常骨更脆弱。骨佩吉特病的并发症可包括骨痛、骨关节炎、骨骼畸形、听力丧失和骨折。本综述的目的是全面概述骨佩吉特病当前的治疗标准。
对1974年至2007年的文献进行了综述,主题包括骨佩吉特病的流行病学、病因、治疗以及双膦酸盐类药物。
在北美和西欧,估计55岁及以上人群中有2% - 7%患有骨佩吉特病。双膦酸盐类药物的抗吸收治疗是标准治疗方法,但口服治疗可能存在局限性。静脉注射帕米膦酸有效且早已可用,但其使用受到不切实际的推荐给药方案的阻碍,即连续三天每天静脉注射30毫克,持续4小时。在两项相同的、为期6个月的双盲试验中,5毫克唑来膦酸一次性静脉治疗的患者中有96%达到治疗反应,而每日口服30毫克利塞膦酸60天治疗的患者中这一比例为74%(p < 0.001)。本综述的一个局限性是,历史数据的审查细节程度不如新治疗方法,因为骨佩吉特病药物治疗的最新进展降低了旧药物的临床实用性。
骨佩吉特病病因尚不清楚,但一些证据表明存在遗传和病毒因素。双膦酸盐类药物可恢复正常的骨转换并缓解骨痛,但口服制剂可能因给药方案复杂和胃肠道吸收差而受到限制。双膦酸盐类药物唑来膦酸通过单次静脉输注给药,具有抗吸收疗效且缓解期更长。